Archive

[vc_text_separator title="PRESENTATION ABOUT SIGMATECH 3.0 SOFTWARE"][vc_empty_space height="16px"][vc_gallery type="nivo" interval="3" images="6831,6832,6833,6834,6835,6836,6837,6838,6839,6840,6841,6842,6843,6844,6845,6846,6847,6848,6849,6850,6851,6852,6853,6854,6855,6856,6857,6858,6859,6860,6861,6862,6868" img_size="full"][vc_empty_space height="16px"]  SigmaTech 3.1     SigmaTech 3.1  is a software for achieving objectives of QbD. It is useful for Designing and building quality into the process using DOE technique. The statistically planned experimental data will be analysed by this software to build the statistical/mathematical model and provide various simulation techniques for optimal design of the process.  This software is...

Hostrin Life Sciences associated with various dedicated R&D, FR&D and Analytical development teams including stability study's for the new product development of intermediates, API's, Formulations, Bio technology, Bio similars, Transdermal patches with infringing and non infringing routes which leads to file DMF, CTD, ACTD, eCTD and NDA/ANDA  with all therapeutics exclusively Innovative molecules, CRO molecules and ONCOLOGY molecules including marketing authorization (MA). After product development we...

Registration of Dossier for the pharmaceutical product is a document that contains all the technical data (administrative, quality, nonclinical and clinical) which has to be approved / registered / marketed in a country. It is more commonly called as the New Drug Application (NDA) in the USA or Marketing Authorization Application (MAA) in the European Union (EU) and other countries, or simply Registration Dossier. Basically,...